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rs397517912

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517912(A;A)
Make rs397517912(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156135244
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517912
ebirs397517912
HLIrs397517912
Exacrs397517912
Varsomers397517912
Maprs397517912
PheGenIrs397517912
hapmaprs397517912
1000 genomesrs397517912
hgdprs397517912
ensemblrs397517912
gopubmedrs397517912
geneviewrs397517912
scholarrs397517912
googlers397517912
pharmgkbrs397517912
gwascentralrs397517912
openSNPrs397517912
23andMers397517912
23andMe allrs397517912
SNP Nexus

SNPshotrs397517912
SNPdbers397517912
MSV3drs397517912
GWAS Ctlgrs397517912
Max Magnitude0
ClinVar
Risk rs397517912(A;A)
Alt rs397517912(A;A)
Reference rs397517912(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene LMNA
CLNDBN not specified not provided
Reversed 0
HGVS NC_000001.10:g.156105035G>A
CLNSRC
CLNACC RCV000041376.2, RCV000235283.1,